Experimental and Numerical Determination of Thermal Radiative Properties of ZnO Particulate Media

Author(s):  
Patrick Coray ◽  
Wojciech Lipin´ski ◽  
Aldo Steinfeld

The radiative characteristics of packed beds of ZnO particles, applied in the design of high-temperature solar thermochemical reactors, were investigated experimentally. ZnO samples of varying thickness were exposed to a continuous beam of near monochromatic thermal radiation in the 0.5–1 μm wavelength range. The overall transmitted fraction measured as a function of sample thickness s obeys an exponential trend exp(–As), with the fit parameter A ranging from (4000 ± 100) m−1 at 555 nm to (2100 ± 100) m−1 at 1 μm. In the forward directions, the measured intensity distribution is approximately isotropic, whereas in the backward directions it is well approximated by a Henyey–Greenstein equation with asymmetry factor g ≈ − 0.4 at 555 nm and g ≈ − 0.1 at 1 μm. A Monte Carlo ray-tracing model of the experimental set-up is employed to extract the extinction coefficient and the scattering albedo for the case of non-grey absorbing-scattering medium.

2009 ◽  
Vol 132 (1) ◽  
Author(s):  
P. Coray ◽  
W. Lipiński ◽  
A. Steinfeld

The radiative characteristics of dependently scattering packed-beds of ZnO particles, applied in the design of high-temperature solar thermochemical reactors, were investigated experimentally. ZnO samples of varying thickness were exposed to a continuous beam of near monochromatic thermal radiation in the 0.5–1 μm wavelength range. The overall transmitted fraction measured as a function of sample thickness s obeys an exponential trend exp(−As), with the fit parameter A ranging from 4000±100 m−1 at 555 nm to 2100±100 m−1 at 1 μm. In the forward directions, the measured intensity distribution is approximately isotropic, whereas in the backward directions it is well approximated by a Henyey–Greenstein equation with asymmetry factors g≈−0.4 at 555 nm and g≈−0.1 at 1 μm. A Monte Carlo ray-tracing model of the experimental setup is employed to extract the extinction coefficient and the scattering albedo for the case of a nongray absorbing-scattering medium.


2009 ◽  
Vol 48 (8) ◽  
pp. 1510-1516 ◽  
Author(s):  
Klaus Jäger ◽  
Wojciech Lipiński ◽  
Helmut G. Katzgraber ◽  
Aldo Steinfeld

Author(s):  
Douglas L. Dorset

The quantitative use of electron diffraction intensity data for the determination of crystal structures represents the pioneering achievement in the electron crystallography of organic molecules, an effort largely begun by B. K. Vainshtein and his co-workers. However, despite numerous representative structure analyses yielding results consistent with X-ray determination, this entire effort was viewed with considerable mistrust by many crystallographers. This was no doubt due to the rather high crystallographic R-factors reported for some structures and, more importantly, the failure to convince many skeptics that the measured intensity data were adequate for ab initio structure determinations.We have recently demonstrated the utility of these data sets for structure analyses by direct phase determination based on the probabilistic estimate of three- and four-phase structure invariant sums. Examples include the structure of diketopiperazine using Vainshtein's 3D data, a similar 3D analysis of the room temperature structure of thiourea, and a zonal determination of the urea structure, the latter also based on data collected by the Moscow group.


Author(s):  
Kjersti Gjønnes ◽  
Jon Gjønnes

Electron diffraction intensities can be obtained at large scattering angles (sinθ/λ ≥ 2.0), and thus structure information can be collected in regions of reciprocal space that are not accessable with other diffraction methods. LACBED intensities in this range can be utilized for determination of accurate temperature factors or for refinement of coordinates. Such high index reflections can usually be treated kinematically or as a pertubed two-beam case. Application to Y Ba2Cu3O7 shows that a least square refinememt based on integrated intensities can determine temperature factors or coordinates.LACBED patterns taken in the (00l) systematic row show an easily recognisable pattern of narrow bands from reflections in the range 15 < l < 40 (figure 1). Integrated intensities obtained from measured intensity profiles after subtraction of inelastic background (figure 2) were used in the least square fit for determination of temperature factors and refinement of z-coordinates for the Ba- and Cu-atoms.


1996 ◽  
Vol 33 (1) ◽  
pp. 311-323 ◽  
Author(s):  
A. Witteborg ◽  
A. van der Last ◽  
R. Hamming ◽  
I. Hemmers

A method is presented for determining influent readily biodegradable substrate concentration (SS). The method is based on three different respiration rates, which can be measured with a continuous respiration meter which is operated in a cyclic way. Within the respiration meter nitrification is inhibited through the addition of ATU. Simulations were used to develop the respirometry set-up and decide upon the experimental design. The method was tested as part of a large measurement programme executed at a full-scale plant. The proposed respirometry set-up has been shown to be suitable for a semi-on-line determination of an influent SS which is fully based on the IAWQ #1 vision of the activated sludge process. The YH and the KS play a major role in the principle, and should be measured directly from the process.


1989 ◽  
Vol 54 (7) ◽  
pp. 1785-1794 ◽  
Author(s):  
Vlastimil Kubáň ◽  
Josef Komárek ◽  
Zbyněk Zdráhal

A FIA-FAAS apparatus containing a six-channel sorption equipment with five 3 x 26 mm microcolumns packed with Spheron Oxin 1 000, Ostsorb Oxin and Ostsorb DTTA was set up. Combined with sorption from 0.002M acetate buffer at pH 4.2 and desorption with 2M-HCl, copper can be determined at concentrations up to 100, 150 and 200 μg l-1, respectively. For sample and eluent flow rates of 5.0 and 4.0 ml min-1, respectively, and a sample injection time of 5 min, the limit of copper determination is LQ = 0.3 μg l-1, repeatability sr is better than 2% and recovery is R = 100 ± 2%. The enrichment factor is on the order of 102 and is a linear function of time (volume) of sample injection up to 5 min and of the sample injection flow rate up to 11 ml min-1 for Spheron Oxin 1 000 and Ostsorb DTTA. For times of sorption of 60 and 300 s, the sampling frequency is 70 and 35 samples/h, respectively. The parameters of the FIA-FAAS determination (acetylene-air flame) are comparable to or better than those achieved by ETA AAS. The method was applied to the determination of traces of copper in high-purity water.


1996 ◽  
Vol 61 (6) ◽  
pp. 844-855 ◽  
Author(s):  
Olga Šolcová ◽  
Petr Schneider

It was shown that the sampling loop, detector and connecting elements in the chromatographic set-up for determination of transport parameters by the dynamic method significantly influence the response peaks from columns packed with porous or nonporous particles. A method, based on the use of convolution theorem, was developed which can take these effects into account. The applicability of this method was demonstrated on the case of axial dispersion in a single-pellet-string column (SPSR) packed with nonporous particles. It is possible to handle also responses from columns packed with porous particles by a similar procedure.


Sign in / Sign up

Export Citation Format

Share Document